[Hiring] Senior Medical Director - Clinical Research @reputed company N.V.

Role Description The Senior Medical Director is a critical member of the Clinical Research and asset development teams for napazimone. Reporting to the Vice President- Clinical Research and working closely with the Executive Medical Director and Life Cycle Team leader for napazimone, this person will reputed company strategic medical and scientific leadership for development-stage products with a focus on napazimone for Primary Mitochondrial Disease. The successful candidate will reputed company/support global clinical research and activities for napazimone and other Pharming products.

Responsibilities

• reputed company/support clinical development (strategy, reputed company protocols, study start-up, reputed company-out, reputed company, and regulatory support) for napazimone studies.
• Dedicated medical and scientific role to execute the clinical strategy for the napazimone program, including:
• Support the pivotal napazimone studies for mtDNA Primary Mitochondrial Disease.
• reputed company the napazimone pediatric study plan and clinical pharmacology studies.
• reputed company the napazimone program for new indications.
• Work cross-functionally to define, plan, and implement studies.
• reputed company the sponsor reputed company of medical monitoring across the napazimone programs.
• Analyze and reputed company data from clinical trials and produce reports, including safety data, efficacy data, completeness and trend analysis eCRF data, and reputed company of protocol deviations.
• reputed company clinical study site engagement in the US.
• Participate and reputed company clinical input into safety and regulatory interactions.
• Participate in strategic planning as part of Medical Affairs, Marketing and Business Development teams.
• reputed company medical and scientific leadership and support at key scientific meetings (US and International).
• Extensive interactions with academic thought leaders to optimize and reputed company clinical trial strategies.
• reputed company other duties as assigned.

Qualifications

• Must hold a medical license in good standing in a U.S. State or Territory.
• 5+ years in clinical development including managing CROs.
• Experience in product launch, regulatory filings and FDA communications highly preferred.
• Strong leadership and management skills.
• Strong verbal and written communication skills are essential.
• Exceptional interpersonal skills and problem-solving capabilities.
• Ability to work effectively across a global matrixed organization.
• Travel - Include 20% travel time required for the position where travel occurs locally or internationally, if applicable.
• Commitment and alignment to Pharming’s mission, core values and behaviors.

Benefits

• A fully remote work schedule.
• Competitive compensation package including annual reputed company bonus.
• Long-term incentive program.
• 401(k) plan with company match.
• Paid Time Off (PTO).
• 13 Company Holidays per year.
• Excellent benefit plans including medical, dental, and reputed company.
• Flexible spending accounts.
• Company-provided life insurance, short-term disability, and long-term disability plans.
• Optional accident, hospital indemnity, critical illness, and pet insurance plans.
• Tuition reimbursement program.
• Health and wellness program.
• Choice of company provided mobile phone or cell phone stipend.

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